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PubMed:8605116 JSONTXT

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DisGeNET

Id	Subject	Object	Predicate	Lexical cue
T0	26-29	gene:5925	denotes	RB1
T1	52-77	disease:C0751483	denotes	hereditary retinoblastoma
R1	T0	T1	associated_with	RB1,hereditary retinoblastoma

DisGeNET5_gene_disease

Id	Subject	Object	Predicate	Lexical cue
8605116-0#26#29#gene5925	26-29	gene5925	denotes	RB1
8605116-0#52#77#diseaseC0751483	52-77	diseaseC0751483	denotes	hereditary retinoblastoma
8605116-1#61#64#gene5925	140-143	gene5925	denotes	RB1
8605116-1#94#118#diseaseC0854914	173-197	diseaseC0854914	denotes	bilateral retinoblastoma
26#29#gene592552#77#diseaseC0751483	8605116-0#26#29#gene5925	8605116-0#52#77#diseaseC0751483	associated_with	RB1,hereditary retinoblastoma
61#64#gene592594#118#diseaseC0854914	8605116-1#61#64#gene5925	8605116-1#94#118#diseaseC0854914	associated_with	RB1,bilateral retinoblastoma

NCBIDiseaseCorpus

Id	Subject	Object	Predicate	Lexical cue
T1	52-77	SpecificDisease:D012175	denotes	hereditary retinoblastoma
T2	152-197	CompositeMention:D012175	denotes	familial or sporadic bilateral retinoblastoma

ncbi-valid

Id	Subject	Object	Predicate	Lexical cue
T1	52-77	SpecificDisease	denotes	hereditary retinoblastoma
T2	152-197	CompositeMention	denotes	familial or sporadic bilateral retinoblastoma

ncbi-valid-gpt-nr-ng

Id	Subject	Object	Predicate	Lexical cue
T1	52-77	SpecificDisease	denotes	hereditary retinoblastoma
T2	152-197	CompositeMention	denotes	familial or sporadic bilateral retinoblastoma

ncbi-valid-gpt-nr-g

Id	Subject	Object	Predicate	Lexical cue
T1	52-77	SpecificDisease	denotes	hereditary retinoblastoma
T2	152-197	CompositeMention	denotes	familial or sporadic bilateral retinoblastoma

ncbi-valid-gpt-r-g

Id	Subject	Object	Predicate	Lexical cue
T1	52-77	SpecificDisease	denotes	hereditary retinoblastoma
T2	152-197	CompositeMention	denotes	familial or sporadic bilateral retinoblastoma

ncbi-valid-gpt-r-ng

Id	Subject	Object	Predicate	Lexical cue
T1	52-77	SpecificDisease	denotes	hereditary retinoblastoma
T2	152-197	CompositeMention	denotes	familial or sporadic bilateral retinoblastoma

ncbi-valid-gemini-nr-ng

Id	Subject	Object	Predicate	Lexical cue
T1	52-62	Modifier	denotes	hereditary
T2	63-77	SpecificDisease	denotes	retinoblastoma
T3	183-197	SpecificDisease	denotes	retinoblastoma

ncbi-valid-gemini-r-g

Id	Subject	Object	Predicate	Lexical cue
T1	52-77	SpecificDisease	denotes	hereditary retinoblastoma
T2	152-197	CompositeMention	denotes	familial or sporadic bilateral retinoblastoma

ncbi-valid-gemini-nr-g

Id	Subject	Object	Predicate	Lexical cue
T1	52-77	SpecificDisease	denotes	hereditary retinoblastoma
T2	183-197	SpecificDisease	denotes	retinoblastoma

ncbi-valid-deepseek-nr-ng

Id	Subject	Object	Predicate	Lexical cue
T1	0-18	Modifier	denotes	Germline mutations
T2	26-29	SpecificDisease	denotes	RB1
T3	52-77	CompositeMention	denotes	hereditary retinoblastoma
T4	140-143	SpecificDisease	denotes	RB1
T5	173-197	CompositeMention	denotes	bilateral retinoblastoma
T6	459-462	DiseaseClass	denotes	PCR
T7	500-503	DiseaseClass	denotes	PCR

ncbi-valid-deepseek-nr-g

Id	Subject	Object	Predicate	Lexical cue
T1	52-77	SpecificDisease	denotes	hereditary retinoblastoma
T2	164-197	SpecificDisease	denotes	sporadic bilateral retinoblastoma

ncbi-valid-deepseek-r-ng

Id	Subject	Object	Predicate	Lexical cue
T1	52-62	Modifier	denotes	hereditary
T2	63-77	SpecificDisease	denotes	retinoblastoma
T3	152-160	Modifier	denotes	familial
T4	164-172	Modifier	denotes	sporadic
T5	173-182	Modifier	denotes	bilateral
T6	183-197	SpecificDisease	denotes	retinoblastoma

ncbi-valid-deepseek-r-g

Id	Subject	Object	Predicate	Lexical cue
T1	52-77	SpecificDisease	denotes	hereditary retinoblastoma
T2	152-197	CompositeMention	denotes	familial or sporadic bilateral retinoblastoma

ncbi-valid-gemini-r-ng

Id	Subject	Object	Predicate	Lexical cue
T1	52-77	CompositeMention	denotes	hereditary retinoblastoma
T2	152-160	Modifier	denotes	familial
T3	164-172	Modifier	denotes	sporadic
T4	173-182	Modifier	denotes	bilateral
T5	183-197	SpecificDisease	denotes	retinoblastoma

ncbi-valid-gemini-r-m

Id	Subject	Object	Predicate	Lexical cue
T1	52-77	SpecificDisease	denotes	hereditary retinoblastoma
T2	152-197	CompositeMention	denotes	familial or sporadic bilateral retinoblastoma

ncbi-valid-gpt-r-m

Id	Subject	Object	Predicate	Lexical cue
T1	52-77	SpecificDisease	denotes	hereditary retinoblastoma
T2	152-197	CompositeMention	denotes	familial or sporadic bilateral retinoblastoma

ncbi-valid-deepseek-r-m

Id	Subject	Object	Predicate	Lexical cue
T1	52-77	SpecificDisease	denotes	hereditary retinoblastoma
T2	152-197	CompositeMention	denotes	familial or sporadic bilateral retinoblastoma

NCBI-Disease-Develop

Id	Subject	Object	Predicate	Lexical cue	database_id
T340	52-77	SpecificDisease	denotes	hereditary retinoblastoma	D012175
T341	152-197	CompositeMention	denotes	familial or sporadic bilateral retinoblastoma	D012175

NCBI-Disease-Corpus-All

Id	Subject	Object	Predicate	Lexical cue	database_id
T340	52-77	SpecificDisease	denotes	hereditary retinoblastoma	D012175
T341	152-197	CompositeMention	denotes	familial or sporadic bilateral retinoblastoma	D012175

NCBI-Disease-Corpus-2stage-All

Id	Subject	Object	Predicate	Lexical cue
T1	63-77	SpecificDisease	denotes	retinoblastoma
T2	183-197	SpecificDisease	denotes	retinoblastoma

NCBI-Disease-Corpus-rezarta-All

Id	Subject	Object	Predicate	Lexical cue
T1	52-77	SpecificDisease	denotes	hereditary retinoblastoma
T2	183-197	SpecificDisease	denotes	retinoblastoma

NCBI-Disease-Corpus-4oGuideline-All

Id	Subject	Object	Predicate	Lexical cue
T1	52-77	Modifier	denotes	hereditary retinoblastoma
T2	173-197	SpecificDisease	denotes	bilateral retinoblastoma

NCBI-Disease-Corpus-Simple-All

Id	Subject	Object	Predicate	Lexical cue
T1	52-77	SpecificDisease	denotes	hereditary retinoblastoma
T2	183-197	SpecificDisease	denotes	retinoblastoma